Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients suffering from autoimmune diseases. Guided by our core values, Stay True to Why, Collaborate to Accelerate, Lead with Clarity, Boldly Innovative, and Own the Outcome, we are committed to transforming the future of treatment for autoimmune disease. Join us at the forefront of cell therapy innovation and help redefine what’s possible.
Position Overview
Kyverna is seeking an experienced IT Validation Engineer to support the implementation, validation, and lifecycle management of computerized systems across GxP and regulated business functions. ) This role will play a critical hands-on role in executing Kyverna’s Computer Software Assurance (CSA) program, supporting system onboarding, validation deliverables, and vendor/system assessments to ensure compliance with regulatory requirements (e.g., FDA, EMA, 21 CFR Part 11). The ideal candidate thrives in a fast-paced environment, is comfortable owning execution, and can partner cross-functionally with IT, Quality, Clinical, and external vendors ensuring that GxP systems are validated, compliant, and inspection-ready.
Department: IT
Location: Remote eligible
Reports To: Associate Director, IT Compliance